Medical Device Recalls
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1 result found
510(K) Number: K083207 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Ultrawave II EX 1320/ Ultrawave III EX 1320 Powered Laser Surgical Instrument. Nd:YAG 1064 nm: Coag... | 2 | 01/17/2013 | Quanta System, S.p.A. |
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